A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622775



Internal ID7009633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:29560653..29561360hg38UCSC Ensembl
Innerchr10:29560703..29561310hg38UCSC Ensembl
Outerchr10:29560519..29561494hg38UCSC Ensembl
chr10:29849582..29850289hg19UCSC Ensembl
Innerchr10:29849632..29850239hg19UCSC Ensembl
Outerchr10:29849448..29850423hg19UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg38708
hg19708
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13742993, essv13742986, essv13742996, essv13742995, essv13742992, essv13742987, essv13742985, essv13742988, essv13742991, essv13742989, essv13742998, essv13742997, essv13742990, essv13742994, essv13742999
SamplesHG03812, HG03009, HG04059, HG03911, HG03784, HG03709, HG03786, HG04177, HG04173, HG03695, HG03692, HG03896, NA21101, HG03864, HG04198
Known GenesSVIL
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622775
Frequency
Sample Size2504
Observed Gain0
Observed Loss15
Observed Complex0
Frequencyn/a


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